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Differential Mechanism of Action of 3,4',7-O-trimethylquercetin in Three Types of Ovarian Cancer Cells
- Source :
- Anticancer research. 38(9)
- Publication Year :
- 2018
-
Abstract
- Background/aim 3,4',7-O-trimethylquercetin (34'7TMQ), a derivative of quercetin, inhibited ovarian cancer cell migration and invasion without affecting proliferation. In this study, the apoptotic effect of 34'7TMQ on three cancer cell lines (CRL-1978, CRL-11731, SK-OV-3) was evaluated. Materials and methods Expression of pro-apoptotic proteins such as Bax/Bcl-2 ratio, p38 MAP kinase, and caspase-9 were measured by western blot analysis. Annexin-V staining was performed to visualize apoptotic signaling. Results Caspase-9 was up-regulated in all three cell lines. Bax/Bcl-2 ratio was up-regulated in CRL-1978 and SK-OV-3 but down-regulated in CRL-11731. The p38 MAPK was down-regulated in CRL-1978, up-regulated in SK-OV-3, and had differential expression in CRL-11731. Annexin V staining indicated that 34'7TMQ at 6.25 μM induced apoptotic signaling in the CRL-1978 ovarian cancer cell line. Conclusion 34'7TMQ induced apoptosis in three types of cancer cell lines but it appears to have a different mechanism of action in each cell line.
- Subjects :
- 0301 basic medicine
Cancer Research
Cell Survival
Down-Regulation
p38 Mitogen-Activated Protein Kinases
03 medical and health sciences
0302 clinical medicine
Western blot
Annexin
Cell Movement
Cell Line, Tumor
medicine
Humans
Ovarian Neoplasms
medicine.diagnostic_test
biology
Chemistry
fungi
food and beverages
Cell migration
General Medicine
medicine.disease
Antineoplastic Agents, Phytogenic
Gene Expression Regulation, Neoplastic
030104 developmental biology
Oncology
Mechanism of action
Apoptosis
Cell culture
030220 oncology & carcinogenesis
Mitogen-activated protein kinase
Cancer research
biology.protein
Female
Quercetin
medicine.symptom
Ovarian cancer
Apoptosis Regulatory Proteins
Subjects
Details
- ISSN :
- 17917530
- Volume :
- 38
- Issue :
- 9
- Database :
- OpenAIRE
- Journal :
- Anticancer research
- Accession number :
- edsair.doi.dedup.....4b586d229772fc2100b0ccf475ad6edd